Actively Recruiting
Correlation of FFR CT With Invasive FFR in Multi-ethnic Cohort- a Retrospective Study
Led by Sandwell & West Birmingham Hospitals NHS Trust · Updated on 2026-05-07
500
Participants Needed
1
Research Sites
30 weeks
Total Duration
On this page
Sponsors
S
Sandwell & West Birmingham Hospitals NHS Trust
Lead Sponsor
A
Aston University
Collaborating Sponsor
AI-Summary
What this Trial Is About
This study aims to examine the correlation between Fractional Flow Reserve (FFR) FFR Computed Tomography (CT) and invasive FFR in a real-world setting using retrospective analysis of existing data, providing practical insights directly applicable to patient care. By confirming or examining the accuracy of FFR CT in a clinical setting, our analysis could support its broader adoption as a routine non-invasive diagnostic tool potentially (a) reducing the need for invasive testing (b) minimising associated risks, and(c) lowering healthcare costs and provide fresh insights into non-invasive coronary diagnostics. Our findings will also help understand the relevance of these tests across different ethnic groups and the population we serve.
CONDITIONS
Official Title
Correlation of FFR CT With Invasive FFR in Multi-ethnic Cohort- a Retrospective Study
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 18 years or older
- Stable patients with suspected coronary artery disease
- Patients who underwent CT coronary angiography (CTCA), FFR CT, and invasive FFR
- CTCA images must be high quality with clear visualization of coronary arteries and minimal artifacts
You will not qualify if you...
- Younger than 18 years of age
- Did not undergo FFR CT
- CT coronary angiography images of inadequate quality or degraded
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Sandwell and West Birmingham NHS Trust
Birmingham, West Midlands, United Kingdom, B71 4HJ
Actively Recruiting
Research Team
V
Vinoda Sharma, FRCP FESC FRCPE
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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